VAERS 2021 Database www.vaers.hhs.gov

Main Page | All 2021 Deaths | Videos
VAERS Updated: 10/01/2021
** VAERS DATABASE Last updated: October 1, 2021**
PLEASE CHECK BACK SOON
Download the files above while you wait.






Manufacturers

Total Manufacturer
187,133MODERNA
33,878JANSSEN
2,321PFIZER\BIONTECH
1,091GLAXOSMITHKLINE BIOLOGICALS
983UNKNOWN MANUFACTURER
363MERCK & CO. INC.
229SEQIRUS, INC.
45DYNAVAX TECHNOLOGIES CORPORATION
41NOVARTIS VACCINES AND DIAGNOSTICS
29SANOFI PASTEUR
18EMERGENT BIOSOLUTIONS
8PAXVAX
7TEVA PHARMACEUTICALS
4PFIZER\WYETH
3BERNA BIOTECH, LTD.
2SMITHKLINE BEECHAM
2INTERCELL AG
2PROTEIN SCIENCES CORPORATION
1CSL LIMITED

Incidents per State

State Total
77,548
AK1,869
AL5,581
AR3,688
AS47
AZ14,288
CA61,984
CO11,665
CT8,149
DC1,663
DE1,807
FL37,749
FM5
GA15,058
GU120
HI2,453
IA4,625
ID2,692
IL20,334
IN24,007
KS4,615
KY7,696
LA4,887
MA14,654
MD12,514
ME3,129
MH11
MI18,739
MN12,528
MO9,710
MP29
MS2,790
MT2,375
NC16,368
ND1,356
NE2,880
NH3,100
NJ17,634
NM3,916
NV4,239
NY34,355
OH19,081
OK6,195
OR8,636
PA23,083
PR2,370
QM2
RI2,088
SC6,411
SD1,212
TN9,131
TX35,174
UT4,273
VA14,937
VI64
VT1,676
WA14,909
WI11,259
WV2,388
WY861
XB5
XL1
XV2

ID: 1306060
Sex: M
Age:
State: CO

Vax Date:
Onset Date:
Rec V Date: 05/11/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot: 037K20A
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data:

Allergies:

Symptom List: Dysphagia, Epiglottitis

Symptoms: Migraine; light sensitive; Extremely nauseous; Extremely dizzy; Headache; This is a spontaneous report from a contactable consumer. This consumer reported similar events for herself and her husband. This is 2nd of 2 reports. A male patient of an unspecified age received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on an unspecified date (Batch/Lot number was not reported) as single dose for Covid-19 immunization. The patient's medical history and concomitant medications were not reported. On an unspecified date, the patient experienced migraine, light sensitive, extremely nauseous, extremely dizzy, and headache but he was able to sleep at night. (These events were reported as "similar side effects" with the patient's spouse.). The outcome of events was unknown. Information on the lot/batch number has been requested.; Sender's Comments: Linked Report(s) : US-PFIZER INC-2021477842 same reporter, drug, and event, different patient

Other Meds:

Current Illness:

ID: 1306061
Sex: F
Age:
State: MA

Vax Date: 04/28/2021
Onset Date: 04/01/2021
Rec V Date: 05/11/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot: 025L20A
Dose Series: 1
Vax Route: IM
Vax Site: RA

Lab Data:

Allergies:

Symptom List: Anxiety, Dyspnoea

Symptoms: fever; This is a spontaneous report from a Pfizer sponsored program COVAX US support. A contactable consumer (Patient) reported two reports for herself and her son. This is one of the two reports. A 52-year-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number and expiry date were not reported), via an unspecified route of administration on 28Apr2021 as single dose for covid-19 immunization. The patient medical history and concomitant medications were not reported. The patient received the 2nd dose of the Pfizer covid vaccine yesterday on 28Apr2021. She and her son have a fever in Apr2021. Caller also stated 'Tylenol' didn't really work for her. The outcome of the event was unknown. No follow-up attempts are needed; information about lot/batch number cannot be obtained.; Sender's Comments: Linked Report(s) : US-PFIZER INC-2021481479 same reporter, product and AE, different patient

Other Meds:

Current Illness:

ID: 1306062
Sex: F
Age:
State: IL

Vax Date: 03/11/2021
Onset Date:
Rec V Date: 05/11/2021
Hospital:

Vax Type: COVID19
Manufacturer: PFIZER\BIONTECH
Vax Name: COVID19 (COVID19 (PFIZER-BIONTECH))
Lot: EL1284
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data:

Allergies:

Symptom List: Chest discomfort, Dysphagia, Pain in extremity, Visual impairment

Symptoms: muscle pain increased after the second dose; her anxiety increased after the second dose; This is a spontaneous report from a contactable consumer (patient) via a Pfizer-sponsored program COVAX US Support. A female patient of an unspecified age received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, lot number and expiration date were not provided) via an unspecified route of administration on 11Mar2021 as a single dose for COVID-19 immunisation. Medical history included spinal cord disorder, anxiety, muscle pain and breast cancer (survivor for 33 years). Concomitant medications included blood pressure (unspecified),blood thinner (unspecified), pain medication and anxiety medication. Patient historical vaccine included first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, lot number and expiration date were not provided) via an unspecified route of administration on 12Feb2021 as a single dose for COVID-19 immunization and experienced injection site swelling. On an unspecified date in 2021, patient had anxiety and muscle pain increased after the second dose. The patient wanted to know if other people experienced the same adverse reaction as she did. The outcome for the events were unknown. No follow-up attempts are needed. No further information is expected.

Other Meds:

Current Illness: Anxiety; Breast cancer (breast cancer survivor for 33 years.); Muscle pain

ID: 1306063
Sex: F
Age:
State: CT

Vax Date: 04/23/2021
Onset Date: 04/24/2021
Rec V Date: 05/11/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot: unknown
Dose Series: UNK
Vax Route:
Vax Site:

Lab Data:

Allergies:

Symptom List: Dizziness, Fatigue, Mobility decreased

Symptoms: felt dizzy; Headache; she had chill; This is a spontaneous report from a contactable consumer (patient) received from Pfizer sponsored program. A female patient of unspecified age received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection, Lot number: unknown), dose 2 via an unspecified route of administration on 23Apr2021, as single dose for COVID-19 immunisation. The patient's medical history and concomitant medications were not reported. The patient previously received first dose of bnt162b2 on an unspecified date. On 24Apr2021 (Saturday), the patient experienced chills. On 25Apr2021 (Sunday), she had a very light headache. On 26Apr2021 (Monday), she had a severe headache and felt dizzy. The outcome of the events was unknown. No follow-up attempts are needed. Information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1306064
Sex: F
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 05/11/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot:
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data:

Allergies:

Symptom List: Injection site erythema, Injection site pruritus, Injection site swelling, Injection site warmth

Symptoms: she felt very sick; chills; fever; This is a spontaneous report received from a Pfizer sponsored program COVAX US Support. A non-contactable consumer (patient) reported for herself that a female patient of an unspecified age received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, solution for injection, Batch/Lot number was not reported), via an unspecified route of administration on an unspecified date at single dose for COVID-19 immunization. The patient medical history includes that she had tested positive to COVID before receiving the 1st vaccine. The concomitant medications were not reported. Caller wanted to know was it ok not to show up for her 2nd appointment because after receiving her 1st dose of the vaccine she felt very sick and had the chills and fever on an unspecified date. At home she took her temperature and it was 99 but when she went to the doctor office it was 97. She read online that she didn't really need the 2nd dose or the vaccine if she already tested positive for COVID. The patient underwent lab tests and procedures which included body temperature: 99, body temperature: 97, SARS-CoV-1 test positive: positive on an unspecified date. The outcome of events was unknown. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1306065
Sex: F
Age:
State:

Vax Date: 04/04/2021
Onset Date:
Rec V Date: 05/11/2021
Hospital:

Vax Type: FLUC4
Manufacturer: SEQIRUS, INC.
Vax Name: INFLUENZA (SEASONAL) (FLUCELVAX QUADRIVALENT)
Lot: 276563
Dose Series: 1
Vax Route: SYR
Vax Site: LA

Lab Data:

Allergies:

Symptom List: Chills, Confusional state, Eye inflammation, Headache, Laboratory test

Symptoms: lymph level is extremely high/Elevated Lymph levels on blood work; This is a spontaneous report from a contactable consumer (patient) reported for herself. A female patient (unknown age) received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, Lot number: unknown, Expiry date: unknown) via an unspecified route of administration, administered at an unspecified anatomical location on 04Apr2021 as SINGLE DOSE for COVID-19 immunization. Patient's medical history and concomitant medications were not reported. On an unspecified date patient had her lab work done and her lymph level was extremely high. Elevated Lymph levels on blood work. The response which the patient received included a review of the prescribing Information for Pfizer Covid Vaccine did not find information regarding elevated lymph. As the Prescribing Information did not include all adverse reactions that have been reported or that may occur, the patient was advised to consult with her doctor/healthcare provider about what she had experienced/experiencing. Because her doctor/healthcare provider is most familiar with her medical condition, clinical history, how her treatment has been conducted and any relevant information to her specific case, her doctor/healthcare provider was in the best position to advise her about the appropriate action to take. The outcome of the event was unknown. No follow-up attempts are needed; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1306066
Sex: F
Age:
State:

Vax Date: 04/15/2021
Onset Date:
Rec V Date: 05/11/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot: 011J20A
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data:

Allergies:

Symptom List: Pyrexia, White blood cell count decreased

Symptoms: sinus infection; asking if Doxycycline with interfere or interact with the vaccine; This is a spontaneous report from a contactable consumer (Patient). A female patient of an unspecified age received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE,/Lot number: not reported), dose 1 via an unspecified route of administration on 15Apr2021 at SINGLE DOSE for covid-19 immunisation. The patient medical history was not reported. on an unspecified date,the patient experienced sinus infection, asking if doxycycline with interfere or interact with the vaccine. Question: Caller is a consumer, asking if Doxycycline with interfere or interact with the vaccine. Caller reports that she received her first vaccine dose on 15Apr2021 and is scheduled for her second dose on 05May2021 but since her first dose she has been diagnosed with a sinus infection and was prescribed Doxycycline antibiotic. She reports "I read on the fact sheet that you shouldn't take other vaccines when getting the covid vaccine and I want to know if it is safe to take my antibiotic for 10 days if I'm planning to get my second shot". Caller reports that she already talked to her doctors PA wh'o advised her that it was ok to take the antibiotic, but she stated "He's new and I don't trust him yet". Caller also asks "When can I restart my other medicine" reporting that she was advised to hold her medications, no specific medicine specified, but wasn't told when to restart them. The outcome of the events was unknown. No follow-up attempts are needed; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1306067
Sex: F
Age:
State:

Vax Date: 04/08/2021
Onset Date: 04/08/2021
Rec V Date: 05/11/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot:
Dose Series: UNK
Vax Route: IM
Vax Site: LA

Lab Data:

Allergies:

Symptom List: Pharyngeal swelling

Symptoms: She had diarrhea, vomiting, and stomach pain from the 1st dose; She had diarrhea, vomiting, and stomach pain from the 1st dose; She had diarrhea, vomiting, and stomach pain from the 1st dose; This is a spontaneous report from a contactable consumer (patient). A 56-years-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Batch/Lot number was not reported), dose 1 via an unspecified route of administration on 08Apr2021 (at 56-years age) as single dose for covid-19 immunisation. The patient medical history and concomitant medications were not reported. Patient had diarrhea, vomiting, and stomach pain from the 1st dose and went to doctor on 08Apr2021. They were still ongoing. When patient had blood work done, she had positive antibodies for COVID and the office stated she would have to wait until the end of may to get the second dose. Patient was supposed to get her second dose on 29Apr2021. Patient was asking how she can reschedule her second appointment. The outcome of the event was not recovered. No follow-up attempts are needed; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1306068
Sex: M
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 05/11/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot:
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data:

Allergies:

Symptom List: Abdominal pain, Chills, Sleep disorder

Symptoms: A male patient received both doses of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Lot number: Unknown) via an unspecified route of administration on an unknown date (received second dose day before yesterday as per report) as a single dose for COVID-19 immunization. Medical history was not reported. Concomitant medication included clopidogrel bisulfate (PLAVIX) as an anticoagulant therapy. After both doses, the patient experienced sore arm. Patient was unaware at the time of his injections that he should mention taking an anti-coagulant. The outcome of the event was recovered. No follow-up attempts are needed; information about lot/batch number cannot be obtained.

Other Meds: PLAVIX

Current Illness:

ID: 1306069
Sex: M
Age:
State:

Vax Date: 04/20/2021
Onset Date: 04/01/2021
Rec V Date: 05/11/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot: 011J201A
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data:

Allergies:

Symptom List: Diarrhoea, Nasal congestion

Symptoms: Woke up with chills; Sweat through an undershirt; The arm that they gave the shot in at the injection site got red; Had arthritic stuff in fingers; Late reaction; This is a spontaneous report from a contactable consumer (patient). A male patient (age reported as 77) received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, solution for injection, Lot number and expiration date not reported) via an unspecified route of administration on 20Apr2021 as a single dose for COVID-19 immunisation. Medical history and concomitant medications were not reported. On 26Apr2021, patient blood drawn in general (results unknown). Last night, 28Apr2021 into 29Apr2021 (as reported), the arm that they gave the shot in at the injection site got red. Patient took Tylenol this morning and that subsided. He had arthritic stuff in fingers, but the Tylenol helped and woke up with chills, and his fellow golfers had the chills too, but he also sweat through an undershirt. Patient was scheduled for the second dose on 11May2021 and was just a little anxious of whether to delay it because of a late reaction. The case was non serious. Outcome for the event the arm that they gave the shot in at the injection site got red was recovered on 29Apr2021, had arthritic stuff in fingers was recovering, and for remaining was unknown. No follow-up attempts are needed; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1306070
Sex: F
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 05/11/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot:
Dose Series: 1
Vax Route: SYR
Vax Site: LA

Lab Data:

Allergies:

Symptom List: Vaccination site erythema, Vaccination site pruritus, Vaccination site swelling

Symptoms: muscle and joint aches; muscle and joint aches; teeth and bones hurt; teeth and bones hurt; chills; weakness; I can hardly walk right now; This is a spontaneous report from a contactable consumer (patient) via Medical information team. A 78-year-old female patient received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Lot number: Unknown) via unspecified route of administration on an unspecified date (4 weeks and 2 days after the first dose) (at the age of 78-year) as single dose for COVID-19 immunization. The patient medical history included lumber stenosis. The patient concomitant medications were not reported. Previously patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Lot number: unknown) via unspecified route of administration on unspecified date as single dose for COVID-19 immunization. On an unspecified date, patient felt awful with muscle and joint aches, teeth and bones hurt, chills, weakness. She stated that she could hardly walk right now and could not get over to her primary care physician. The patient informed that she received a steroid injection of some kind on her back for lumbar stenosis 2 weeks and 2 days after the first dose of the vaccine. The outcome of the events was unknown. No follow-up attempts are needed; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1306071
Sex: F
Age:
State: DC

Vax Date: 04/27/2021
Onset Date: 04/28/2021
Rec V Date: 05/11/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot: 039k20a
Dose Series: 1
Vax Route: SYR
Vax Site: RA

Lab Data:

Allergies:

Symptom List: Rash, Urticaria

Symptoms: started experiencing dizziness/vertigo; started experiencing dizziness/vertigo; This is a spontaneous report received from a contactable consumer. A 30-years-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection, Lot Number and Expiration Date was not reported), via an unspecified route of administration on 27Apr2021 as single dose for COVID-19 immunization. The patient medical history and concomitant medications were not reported. It was reported that patient received first dose last Tuesday (on 27Apr2021), starting Wednesday ( on 28Apr2021)afternoon started experiencing dizziness/vertigo. States reported yesterday via phone and ask if this a reported adverse event. The outcome of the events was unknown. No follow-up attempts are needed; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1306072
Sex: F
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 05/11/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot:
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data:

Allergies:

Symptom List: Blood pressure decreased, Chest pain, Chills, Confusional state, Decreased appetite

Symptoms: has not been feeling well; low blood pressure; feeling very cold; clammy; This is a spontaneous report from contactable consumer. This contactable female consumer (Patient) reported for herself. A 52-years-old female patient received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE, Solution for injection, Batch/Lot number was not reported), via an unspecified route of administration on an unspecified date as SINGLE DOSE for COVID-19 immunisation. The patient medical history was not reported. Concomitant medication included metoprolol (METOPROLOL) taken for hypotension, start and stop date were not reported. On an unspecified date She received the first dose on Monday at 07:00PM and had not been feeling well. Patient had been experiencing low blood pressure and feeling very cold and clammy. Patient did not take her heart medication (Metoprolol) because of the low blood pressure. The patient went to the ER but she says they didn't know what to do. No follow-up attempts are needed; information about lot/batch number cannot be obtained.

Other Meds: METOPROLOL

Current Illness:

ID: 1306073
Sex: F
Age:
State:

Vax Date: 04/22/2021
Onset Date: 04/01/2021
Rec V Date: 05/11/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot: 025J20-2A
Dose Series: 1
Vax Route: SYR
Vax Site: LA

Lab Data:

Allergies:

Symptom List: Dyspnoea, Fatigue, Feeling abnormal, Head discomfort, Headache

Symptoms: A female patient received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on 22Apr2021 (Batch/Lot number was not reported) as single dose for COVID-19 immunisation. The patient medical history and concomitant medications were not reported. The patient reported that "she still has bruising at the injection site" on Apr2021 with outcome of unknown. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1306074
Sex: M
Age:
State: NY

Vax Date: 04/09/2021
Onset Date: 04/01/2021
Rec V Date: 05/11/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot: 011J20A
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data:

Allergies:

Symptom List: Heart rate decreased, Heart rate increased, Hypertension, Injection site pain, Musculoskeletal chest pain

Symptoms: A male patient received first dose BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: solution for injection, Batch/Lot number was not reported), via an unspecified route of administration as single dose for COVID-19 immunisation. The patient medical history was not reported. The patient's concomitant medications were not reported. The patient experienced, he noticed a blister on the inside of his mouth on his gums in the front part of his mouth, he states that he punctured it and it drained blood and pus in Apr2021. Patient reported that a few days ago (apprx 25Apr2021) he noticed a blister on the inside of his mouth on his gums in the front part of his mouth. Patient stated that he punctured it and it drained blood and pus and, as of today 29Apr2021, it has resolved and he has no pain. He is going to the Dentist today to have it checked out and states he does not have a current MD to help address his symptom. He reports wearing a bridge. He provided his dentist's contact information. He wanted to know if this side effect could be from the vaccine. There was no PQC. The outcome of event was recovered on 29Apr2021. No follow-up attempts are needed; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1306075
Sex: F
Age:
State:

Vax Date: 04/24/2021
Onset Date: 04/24/2021
Rec V Date: 05/11/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot: 025J20A
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data:

Allergies:

Symptom List: Nausea, Pain, Pain in extremity, Paraesthesia oral, Pyrexia

Symptoms: her armpit got swollen,it is getting worse and is radiating to her back; breast; her armpit got swollen,it is getting worse and is radiating to her back; The caller took the first vaccine on 24Apr2021 and pain started that same day on the same side she was vaccinated; This is a spontaneous report from a contactable consumer or other non hcp. A female patient (consumer) of an unspecified age received bnt162b2 (BNT162B2, Solution for injection), first vaccination dose via an unspecified route of administration on 24Apr2021 (Batch/Lot number was not reported) as SINGLE DOSE for covid-19 immunisation. The patient medical history and concomitant medications were not reported. On 24Apr2021, the patient took first vaccine and pain started that same day on the same side she was vaccinated. After one day on 25Apr2021, her armpit got swollen and then yesterday it came to her breast and it is getting worse and is radiating to her back. The outcome of the events was reported as unknown. No follow-up attempts are needed; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1306076
Sex: F
Age:
State: OH

Vax Date: 01/27/2021
Onset Date:
Rec V Date: 05/11/2021
Hospital:

Vax Type: DTAPHEPBIP
Manufacturer: GLAXOSMITHKLINE BIOLOGICALS
Vax Name: DTAP + HEPB + IPV (PEDIARIX)
Lot:
Dose Series: UNK
Vax Route:
Vax Site: LG

Lab Data:

Allergies:

Symptom List: SARS-CoV-2 antibody test, SARS-CoV-2 test negative

Symptoms: her eyesight has deteriorated since 09 Jan 2021 from 20/80 to 20/200; This is a spontaneous report from a contactable consumer (patient). A 54-years-old female patient received (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection), dose 1 via an unspecified route of administration on 27Jan2021 (Batch/Lot number unknown) as single dose, dose 2 via an unspecified route of administration on 17Feb2021 (Batch/Lot number unknown) as single dose for covid-19 immunisation. Medical history included (Uveitis) pre-existing condition with her left eye (Fuch's Heterochromic Iritis Cyclitis) for 20 years. Concomitant medication(s) included Humira (The patient received 3 doses of Humira on 25Feb2021, 11Mar2021, and 25Mar2021). She went to the doctor to have surgery on her eye and her eyesight has deteriorated since 09Jan2021 from 20/80 to 20/200. She asked if her deterioration in her eye sight was related to the COVID vaccine. The outcome of the event was reported as unknown. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds: HUMIRA

Current Illness:

ID: 1306077
Sex: F
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 05/11/2021
Hospital:

Vax Type: HIBV
Manufacturer: MERCK & CO. INC.
Vax Name: HIB (PEDVAXHIB)
Lot:
Dose Series: UNK
Vax Route:
Vax Site: LG

Lab Data:

Allergies:

Symptom List: Ear pain, Hypoaesthesia

Symptoms: Joint pain; Inflammation; Redness in her knees; This is a spontaneous report from a contactable consumer (Husband to the Patient). A 46-years-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), dose 2 via an unspecified route of administration on an unspecified date (Batch/Lot number was not reported) as single dose for COVID-19 immunisation. Medical history included interstitial cystitis, an autoimmune disorder that affects her bladder, she has had flair ups in her knees in the past. Concomitant medication(s) included pentosan polysulfate sodium (ELMIRON, 100mg) taken for cystitis interstitial; fluoxetine hydrochloride (PROZAC 20mg) taken for an unspecified indication, for 1-2 decades. The patient previously took first dose of vaccine. It was reported that the patient received the second dose of the Pfizer Covid 19 vaccine several weeks ago. Now, she has been having joint pain, inflammation, and redness in her knees. She saw a Rheumatologist yesterday (28Apr2021) who scanned her knee, which found "no water in the knee", and drew labs that were pending. She has had flair ups in her knees in the past. Stated that his wife took the booster shot of the Covid Vaccine several weeks ago. Stated his wife takes other prescription medications as well. They wanted to know if Elmiron was considered an immunosuppressant medication or not, whether her medications could interact with the vaccine and cause the symptoms she is experiencing. Referred caller to HCP for guidance. Outcome of the events was unknown. No follow-up attempts are needed; information about lot/batch number cannot be obtained.

Other Meds: ELMIRON; PROZAC

Current Illness:

ID: 1306078
Sex: F
Age:
State:

Vax Date: 04/21/2021
Onset Date:
Rec V Date: 05/11/2021
Hospital:

Vax Type: PNC13
Manufacturer: PFIZER\WYETH
Vax Name: PNEUMO (PREVNAR13)
Lot:
Dose Series: UNK
Vax Route:
Vax Site: LG

Lab Data:

Allergies:

Symptom List: Abdominal pain upper, Dizziness, Dysgeusia

Symptoms: She had an injury; This is a spontaneous report received from a contactable consumer (reporting on herself). A 35-years-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection, Lot Number and Expiration Date was not reported), via an un-specified route of administration on 21Apr2021 as single dose for COVID-19 immunization. The patient medical history and concomitant medications were not reported. It was reported that patient received the first dose of the BNT162B2 vaccine on 21 April2021. She had an injury and got a medically necessary tetanus shot last night. She understands you are supposed to wait 14 days before and after. she was asking if she able to get the second dose in two weeks. The outcome of the event was unknown. No follow-up attempts are needed; information about lot/batch number cannot be obtained

Other Meds:

Current Illness:

ID: 1306079
Sex: F
Age:
State: OH

Vax Date: 04/27/2021
Onset Date: 04/27/2021
Rec V Date: 05/11/2021
Hospital:

Vax Type: RV1
Manufacturer: GLAXOSMITHKLINE BIOLOGICALS
Vax Name: ROTAVIRUS (ROTARIX)
Lot:
Dose Series: 1
Vax Route: PO
Vax Site: MO

Lab Data:

Allergies:

Symptom List: Blood pressure increased, Chest discomfort, Heart rate increased

Symptoms: Bad migraine; Feels hot; This is a spontaneous report from a Pfizer sponsored program COVAX support via a contactable reporter (patient) reported for herself. A female patient of unspecified age received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection, Lot number: unknown, Expiry date: unknown) via an unspecified route of administration on 27Apr2021 at a single dose for COVID-19 immunisation. The patient's medical history and concomitant medication were not reported. The patient previously took first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection, Lot number: unknown, Expiry date: unknown) via an unspecified route of administration on 06Apr2021 at a single dose for COVID-19 immunisation. No events were reported for the first dose. On 27Apr2021, the caller experienced bad migraine and felt hot after getting the 2nd dose. The outcome of the events was unknown. No follow-up attempts are needed; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1306080
Sex: F
Age:
State: CA

Vax Date: 04/21/2021
Onset Date:
Rec V Date: 05/11/2021
Hospital:

Vax Type: COVID19
Manufacturer: PFIZER\BIONTECH
Vax Name: COVID19 (COVID19 (PFIZER-BIONTECH))
Lot: Eh9899
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data:

Allergies:

Symptom List: Injection site erythema, Injection site pruritus, Injection site swelling, Lymph node pain, Lymphadenopathy

Symptoms: injection site feels sore and tender; had a rash on her arm; arm started to hurt; arm feels like fire; This is a spontaneous report from a contactable consumer (patient herself). A female consumer with unspecified age received second dose of BNT162B2 (COMIRNATY, PFIZER-BIONTECH COVID-19 VACCINE, formulation; solution for injection, lot number/Expiration date) via an unspecified route of administration on 21Apr2021 as single dose for COVID-19 immunisation. The patient medical history and Concomitant medications were not reported. On an unspecified date, Caller stated a week later after received the second dose her arm started to hurt, she had a rash on her arm and the injection site feels sore and tender. As she stated today the rash got bigger, her arm feels like fire. She would like to know if this has been reported and if she should speak to her doctor. Outcome of the event was unknown. No follow-up attempts are needed. Information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1306081
Sex: M
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 05/11/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot:
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data:

Allergies:

Symptom List: Unevaluable event

Symptoms: serious vertigo; exhausted everything I can do; This is a spontaneous report from contactable consumer. This contactable male consumer (Patient) reported that received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE; formulation: solution for injection; Lot number and expiration date were not reported) via an unspecified route of administration, as single dose for COVID-19 immunization.The patient experienced some serious vertigo as a side effect from the vaccine. He reports that he was exhausted everything which he can do and reports that he has seen his HCP who said she had no treatment or fix for him. No follow-up attempts are needed; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1306082
Sex: F
Age:
State:

Vax Date: 04/24/2021
Onset Date: 04/01/2021
Rec V Date: 05/11/2021
Hospital:

Vax Type: COVID19
Manufacturer: PFIZER\BIONTECH
Vax Name: COVID19 (COVID19 (PFIZER-BIONTECH))
Lot:
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data:

Allergies:

Symptom List: Chills, Dizziness, Injection site pain, Myalgia, Pyrexia

Symptoms: Her Legs swelled up again today and it has gotten worse; This is a spontaneous report from a contactable consumer (patient). This contactable female consumer (age not specified) reported for herself that she received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Lot: unknown) through an unspecified route as a single dose on 24Apr2021 (age at vaccination: unknown) for COVID-19 immunization. The patient previously received first dose of BNT162B2 (BNT162B2, Solution for injection, Lot: unknown) and had legs swelled up this lasted for 3 or 4 days and then resolved. After getting her second dose on 24Apr2021 her legs swelled up again today and it had gotten worse. She could not put on shoes or slip-ons. The outcome of event was reported as not resolved. No follow-up attempts are needed; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1306083
Sex: F
Age:
State:

Vax Date: 04/14/2021
Onset Date:
Rec V Date: 05/11/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot: 011L20A
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data:

Allergies:

Symptom List: Injection site pain, Pain

Symptoms: sore throat; This is a spontaneous report from a contactable consumer (Patient herself). A 25-year-old female (non-pregnant )patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, lot number and Expiration date was not reported), via an unspecified route of administration on 14Apr2021 (at the age of 25-year-old) as a single dose for COVID-19 immunization. The patients medical history and concomitant medications were not reported. On an unspecified date the patient reports that's she waking up with a sore throat this morning. The patient did not receive any treatment for the event. The outcome of the event was unknown. No follow-up attempts are needed; information about lot/batch number cannot be obtained

Other Meds:

Current Illness:

ID: 1306084
Sex: F
Age:
State:

Vax Date: 04/13/2021
Onset Date: 04/21/2021
Rec V Date: 05/11/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot:
Dose Series: 1
Vax Route: SYR
Vax Site: LA

Lab Data:

Allergies:

Symptom List: Injection site pain, Menorrhagia

Symptoms: I developed welts, very itchy and blotchy, there was one on my left arm, left side of neck and one big one below my neck or upper back; I developed welts, very itchy and blotchy, there was one on my left arm, left side of neck and one big one below my neck or upper back; I developed welts, very itchy and blotchy, there was one on my left arm, left side of neck and one big one below my neck or upper back; Itchy skin rash, on my right side; This is a spontaneous report from a contactable consumer (patient). This 63-year-old female patient reported that the patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Lot: unknown) via an unspecified route in Left arm as a single dose on 13Apr2021, for covid-19 immunization (age at vaccination: 63). The patient medical history and concomitant medications was not reported. On 21Apr2021, the patient experienced itchy skin rash, on her right side, she had the shot in the left arm. It subsided, then 2 to 3 days later, this past Sunday 25Apr2021 the patient developed welts, very itchy and blotchy, there was one on her left arm, left side of neck and one big one below her neck or upper back. Occurred a week and day after. The clinical outcome of the events was unknown. No follow-up attempts are needed; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1306085
Sex: F
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 05/11/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot: 025J20A
Dose Series: 1
Vax Route: SYR
Vax Site: LA

Lab Data:

Allergies:

Symptom List: Arthralgia, Chills, Headache, Mobility decreased, Myalgia

Symptoms: Her arm is hurting; The pain moved from the arm to arm pit; This is a spontaneous report from a contactable consumer (patient) reporting on herself. A female patient of an unspecified age received BNT162B2(PFIZER-BIONTECH COVID-19 VACCINE, solution for injection), dose 2 via an unspecified route of administration on an unspecified date as single dose for COVID-19 immunisation. The patient's medical history and concomitant medications were not reported. The patient experienced her arm was hurting on an unspecified date and the pain moved from the arm to arm pit on an unspecified. The outcome of both the events was unknown. No follow-up attempts are needed; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1306086
Sex: F
Age:
State: OR

Vax Date:
Onset Date:
Rec V Date: 05/11/2021
Hospital:

Vax Type: COVID19
Manufacturer: PFIZER\BIONTECH
Vax Name: COVID19 (COVID19 (PFIZER-BIONTECH))
Lot:
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data:

Allergies:

Symptom List: Nausea, Pain in extremity, Pyrexia

Symptoms: headache; This is a spontaneous report from a contactable consumer (patient). A 21-year-old female patient received second dose BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, lot number and expiration date were not reported), via an unspecified route of administration on an unspecified date as single dose for COVID-19 immunisation. The patient medical history and concomitant medications were not reported. On an unspecified date, the patient experienced headache After vaccination. The patient asked she received the second dose of the Pfizer-BioNTech COVID-19 vaccine yesterday. she reported a headache to DSU agent, if she could take Aspirin for his symptoms after vaccination. The outcome of the event was unknown. No follow-up attempts are needed; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1306087
Sex: F
Age:
State:

Vax Date: 04/21/2021
Onset Date: 04/21/2021
Rec V Date: 05/11/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot:
Dose Series: UNK
Vax Route: IM
Vax Site: RA

Lab Data:

Allergies:

Symptom List: Chills, Fatigue, Headache, Myalgia

Symptoms: tiredness; Stress; This is a spontaneous report was received from a contactable consumer or other non hcp (patient). A 86-years-old female patient received BNT162B2 ((PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection), dose 2 via an unspecified route of administration on 21Apr2021 (Batch/Lot number was not reported) as single dose for covid-19 immunisation. Medical history included cardiac fibrillation and first BNT162B2 for covid-19 immunisation. The patient's concomitant medications were not reported. The patient received her 2nd dose of the Pfizer covid vaccine on 21Apr2021. She started to experience tiredness on the 27Apr2021 just over a week after the injection. A week after the injection can it cause extreme tiredness? Can it be that far out? The patient had afib (as reported) and had a call out to her cardiologist. Maybe it was stress. The patient did not have anything from the first one. The outcome of the events was unknown. DSU e-transmitting potential duplicate AE. Response: Spoke from EUA PI (LAB-1457-7.0 Revised: 06Apr2021) under section 6 overall safety summary and from attached document No follow-up attempts are needed; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1306088
Sex: F
Age:
State: NY

Vax Date: 04/15/2021
Onset Date: 04/15/2021
Rec V Date: 05/11/2021
Hospital:

Vax Type: COVID19
Manufacturer: PFIZER\BIONTECH
Vax Name: COVID19 (COVID19 (PFIZER-BIONTECH))
Lot:
Dose Series: 1
Vax Route: IM
Vax Site: RA

Lab Data:

Allergies:

Symptom List: Headache, Heart rate increased, Injection site erythema, Injection site pain, Injection site swelling

Symptoms: arm soreness; This is a spontaneous report received from a contactable consumer (patient's husband). A 68-years-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, lot number and expiry date: unknown), via an unspecified route of administration, on 15Apr2021 at 10:30, as single dose for COVID-19 immunisation. Patient's medical history included multiple sclerosis and he had triple bypass surgery three years ago. On 15Apr2021 at 12:00, the patient had soreness. They were sent home with a factsheet for side effects to look out for and to take Tylenol if needed. Outcome of the event was unknown. No follow-up attempts are needed; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1306089
Sex: F
Age:
State:

Vax Date: 04/27/2021
Onset Date: 04/27/2021
Rec V Date: 05/11/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot:
Dose Series: 1
Vax Route: IM
Vax Site: RA

Lab Data:

Allergies:

Symptom List: Nausea

Symptoms: she was loosing her taste and smell; she was loosing her taste and smell; nose constipation; feeling tiredness; generalized body pain; This is a spontaneous report received from a contactable consumer (reporting on herself). A female patient of an unspecified age received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection, Lot Number and Expiration Date was not reported), via an unspecified route of administration on 27Apr2021 as single dose for COVID-19 immunization. The patient medical history and concomitant medications were not reported. Historical vaccine includes first dose of BNT162B2 for COVID-19 immunization. Patient mentions that she got the second dose of the BNT162B2 on 27Apr2021 and that same night she started feeling tiredness and generalized body pain. Next day on 28Apr2021 she continue with the same symptoms but she also noted that she was loosing her taste and smell as well as having nose constipation. She wanted to know if this was normal. The outcome of the events was unknown. No follow-up attempts are needed; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1306090
Sex: F
Age:
State: PA

Vax Date: 04/24/2021
Onset Date: 04/01/2021
Rec V Date: 05/11/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot:
Dose Series: UNK
Vax Route: IM
Vax Site: LA

Lab Data:

Allergies:

Symptom List: Injection site pain

Symptoms: Tingling in her left arm and leg; tested positive 2 weeks ago; This is a spontaneous report from contactable consumer (reported for herself) via Pfizer sponsored program COVAX US support. The female patient of an unspecified age received first dose of BNT162B2 (Pfizer Covid-19 vaccine, solution for injection, Lot number: unknown) via an unspecified route of administration on 24Apr2021 Saturday, as a single dose for Covid-19 immunization. The patient's medical history and concomitant medications were not reported. Two weeks ago, she was tested positive for Covid. On the day of this report, she started noticing more tingling in her left arm and leg. The outcome of the events of positive for Covid and more tingling in her left arm and leg was not reported. No follow-up attempts are needed; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1306091
Sex: M
Age:
State: MN

Vax Date: 04/22/2021
Onset Date:
Rec V Date: 05/11/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot:
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data:

Allergies:

Symptom List: Injection site induration, Injection site pruritus, Injection site swelling, Injection site warmth

Symptoms: Body aches; Cough; Cold; He could resume his vitamin or supplements; scheduled to have his second dose on May 14; Chills; This is a spontaneous report from a contactable consumer (patient) via a Pfizer sponsored program. A 37-year-old male patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, lot number: unknown), via unspecified route of administration on 22Apr2021 as a single dose for COVID-19 immunization. The patient medical history and concomitant medications were not reported. The patient called in to ask if he could resume his vitamin or supplements. The patient received his first dose of the vaccine on 22Apr2021. The patient was scheduled to have his second dose on 14May2021 (which was more than 21 days). The patient specifically asked about vitamins E, C, B, and echinacea, which he states that takes as an immunity booster whenever he feels sick. It was reported that his 37 years old brother received his first dose of the Pfizer BioNTech COVID-19 vaccine and states he has started seeing symptoms of a cold including cough, chills, body aches that continued for 3 days. It was stated that his brother reached out to his doctor who told him it may not be related to the shot but may be because he has come in contact with COVID-19 since his first dose. Caller states that his brother is waiting on a COVID-19 test but caller was concerned because he state that his oxygen levels are going down. The outcome of the events was unknown. No follow-up attempts are needed. Information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1306092
Sex: F
Age:
State:

Vax Date: 01/01/2021
Onset Date: 04/01/2021
Rec V Date: 05/11/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot: 011j20a
Dose Series: 1
Vax Route: IM
Vax Site: RA

Lab Data:

Allergies:

Symptom List: Chills, Dizziness, Nausea, Pain, Tachycardia

Symptoms: arm starting hurting; This is a spontaneous report from a contactable consumer or other non hcp. A 72-years-old female patient received BNT162B2 (BNT162B2), dose 1 via an unspecified route of administration, administered in Arm on Jan2021 (Batch/Lot number was not reported) as single dose, dose 2 via an unspecified route of administration, administered in Arm on 23Feb2021 (Batch/Lot number was not reported) as single dose for covid-19 immunisation. The patient medical history and concomitant medications were not reported. The patient experienced arm starting hurting (pain in extremity), on an unknown date in Apr2021. The patient asked how many people had to report and got response as Stated there have been reports of muscle pain, but it does not specific how long after there vaccination that they felt the pain. The outcome of the event was unknown. No follow-up attempts are possible; Information related to batch/Lot number could not be requested.

Other Meds:

Current Illness:

ID: 1306093
Sex: F
Age:
State: NY

Vax Date: 04/28/2021
Onset Date:
Rec V Date: 05/11/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot: 039K20A
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data:

Allergies:

Symptom List: Tremor

Symptoms: A female patient (unspecified age) received the first dose of BNT162B2 (COMIRNATY, PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection Lot number and expiry date: unknown), via unspecified route on 28Mar2021 at single dose for COVID-19 immunization. On an unspecified date, the patient noticed that when she getting dressed that she had tenderness in a small area that appeared bruised on the bra line to her back on the opposite side from where she got her vaccination. The patient stated that area is small and tender appears to be a "black and blue". The patient also had also had some lethargy, injection site pain and swelling to her arm at the injection site which she understands are normal, but she asks is the bruised area normal. Second dose of vaccination for the patient was scheduled on 19May2021 (21 days apart). The patient did not receive any treatment for the events. Outcome of the events was unknown. The action taken in response to the event(s) for BNT162B2 was not applicable. No follow-up attempts are needed; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1306094
Sex: F
Age:
State:

Vax Date: 04/28/2021
Onset Date:
Rec V Date: 05/11/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot: 025J20A
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data:

Allergies:

Symptom List: Erythema, Pruritus

Symptoms: pain from the shoulder to the fingertips; My whole shoulder; it's been bothering; pain in my arm I woke up with; This is a spontaneous report from a contactable consumer (patient). A 64-years-old female patient received bnt162b2 (BNT162B2), dose 2 via an unspecified route of administration on 28Apr2021 09:30 (Batch/Lot number was not reported) (at the age of -64-year-old) as single dose for covid-19 immunisation. Medical history included, that patient have carpal tunnel pain from an unknown date and was unrelated to getting the vaccine. The patient's concomitant medications were not reported. Patient called on 29Apr2021 and stated she woke up in the middle of the night took a Aleve, as her whole shoulder was been bothering for a week (pain from the shoulder to the fingertips) from pulling weeds/gardening. Patient felt she overdid it. She took 2 Aleve pm 18 hours after the injection and wanted to know if this would ruin the vaccine and whether she need another vaccine. Patient also wanted to know if there is an efficacy detriment. The patient received the 2nd dose of the pfizer covid vaccine yesterday at 9:30am and queried if that taking 2 Aleve tablets effect the vaccine. She also added that she might have taken some Motrin the day before (18 hours prior to getting the vaccine) but was not sure on that. Patient will just get an antibody test after 2 weeks. Patient also confirmed that the vaccine did not bother her at all. She tried to be so careful but because of the pain in my arm she woke up with. The patient was given a response that antibody testing is not recommended to assess for immunity to SARS CoV-2 following COVID-19 vaccination because the clinical utility of post-vaccination testing has not been established. In addition, antibody tests currently authorized under an Emergency Use Authorization (EUA) are not authorized for the assessment of immune response in vaccinated people. The patient took treatment with Aleve (naproxen) as a result of the events. The outcome of the events were reported as unknown. No follow-up attempts are needed; Information related to batch/Lot number could not be requested.

Other Meds:

Current Illness:

ID: 1306095
Sex: F
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 05/11/2021
Hospital:

Vax Type: UNK
Manufacturer: UNKNOWN MANUFACTURER
Vax Name: VACCINE NOT SPECIFIED (NO BRAND NAME)
Lot:
Dose Series: UNK
Vax Route: SYR
Vax Site: UN

Lab Data:

Allergies:

Symptom List: Injection site erythema, Injection site induration, Injection site pruritus, Injection site swelling, Myalgia

Symptoms: She "felt high, like on THC-high"; After her first dose of vaccine, she suffered an injury to her knee; This is a spontaneous report from a contactable consumer (patient). A 56-year-old female patient received the first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Lot number-UNKNOWN) via unspecified route of administration at single dose for COVID-19 immunization. Patient medical history and concomitant medications were not reported. Past drug includes a cortisone shot in her shoulder 6 days before her first dose of the PFIZER BIONTECH COVID-19 VACCINE. After her first dose of vaccine, she suffered an injury to her knee and presented to the orthopedic doctor who declined to give her a cortisone shot in her knee because she was in the middle of the vaccine series. She also mentioned that after her first dose she felt high, like on THC-high and went home and baked chocolate chip cookies- which was out of character for her. The outcome of the events was unknown. No follow-up attempts are needed, information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1306096
Sex: M
Age:
State: OR

Vax Date: 04/26/2021
Onset Date:
Rec V Date: 05/11/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot: 011J20A
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data:

Allergies:

Symptom List: Cough, Limb discomfort, Pain, SARS-CoV-2 test positive

Symptoms: Back pain and Spasm; Back pain and spasm; This is a spontaneous report. A contactable male consumer (patient). A male patient of unspecified age received second dose of (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Solution for injection) via an unspecified route of administration on 26Apr2021 as a single dose for COVID-19 immunisation. The patient's medical history included that the patient had received the fist dose of (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Solution for injection as a single dose for COVID-19 immunisation. The patient's concomitant medications was not reported. The patient experienced back pain and spasm. The outcome of the events was unknown. No follow-up attempts are needed; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1306097
Sex: F
Age:
State:

Vax Date: 04/17/2021
Onset Date: 04/19/2021
Rec V Date: 05/11/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot: 039K20A
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data:

Allergies:

Symptom List: Asthenia, Chills, Headache, Myalgia

Symptoms: she had shingles; she started getting rashes on her back; excruciating pain in her back; This is a spontaneous report from a contactable consumer. A 72-years-old female patient received first dose of BNT162B2 (COMIRNATY, Solution for Injection, Lot number: Unknown, Expiration date: Unknown), at a single dose via unspecified route of administration on 17Apr2021 for COVID-19 immunization. Patient was expected to get the next dose on 08May2021. Medical history and concomitant medications were Unknown. On 19Apr2021 the patient experienced excruciating pain in her back and it lasted for the whole week after two days of vaccination. she visited her doctor, who gave her Celebrex, she started getting rashes on her back on the same day. She was told she had shingles and now she took an antiviral drug. Caller was not transferred due to long wait. She confirmed it was OK to contact her in the evening preferably. Response on the Shingles not found. Spoke per CONS documents below and Referred to her HCP. Outcome of events was reported as unknown. No follow-up attempts are needed; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1306098
Sex: F
Age:
State:

Vax Date: 04/27/2021
Onset Date: 04/28/2021
Rec V Date: 05/11/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot: 011J20A
Dose Series: 1
Vax Route: SYR
Vax Site: LA

Lab Data:

Allergies:

Symptom List: Injection site erythema, Injection site pain, Injection site swelling

Symptoms: I ran a really high Fever yesterday 103.9 F it's back up to 103. F; chills; This is a spontaneous report from a contactable consumer or other non-health care professional. A 48-years-old female patient (consumer) received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection), second vaccination dose via an unspecified route of administration on 27Apr2021 (Batch/Lot number was not reported) as SINGLE DOSE for covid-19 immunization. On an unknown date, patient took first vaccination dose of BNT162B2 (Batch/Lot number was not reported) as SINGLE DOSE for covid-19 immunization. The patient medical history and concomitant medications were not reported. On 28Apr2021 after getting second shot on Tuesday, the patient had ran a really high Fever yesterday 103.9 F it's back up to 103. F and chills were observed with the first 1 to 2 days after vaccination. Patient took Acetaminophen 20 minutes ago and is still pretty high 103 F. On an unknown date, the events were resolved shortly. As per the Clinical Trials Experience Table, Fever which is greater than 38.9 degree C to 40.0 degree C, after second vaccination dose, 1.2 % of patient reported the same event. Outcome of events was resolved. No follow-up attempts are needed; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1306099
Sex: F
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 05/11/2021
Hospital:

Vax Type: COVID19
Manufacturer: PFIZER\BIONTECH
Vax Name: COVID19 (COVID19 (PFIZER-BIONTECH))
Lot: EK9231
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data:

Allergies:

Symptom List: Chills, Feeling cold, Feeling hot, Myalgia, Pain

Symptoms: I had some pain in my arm, not bad though; started itching 2 days after the dose; started itching 2 days after the dose ,"both arms and legs and chest sometimes; This is a spontaneous report from a contactable consumer (patient). A female patient of an unspecified age received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Batch/Lot number and expiry date was not reported), via an unspecified route of administration on an unspecified date as single dose for COVID-19 immunisation. The patient's medical history and concomitant medication was not reported. Patient received her 1st Pfizer vaccine dose and "had some pain in her arm, not bad though" and started itching 2 days after the dose, "both arms and legs and chest sometimes, it would go away and then it would come back." 2nd dose is scheduled on 06May2021. (3 weeks after 1st dose) She had a side effect after the first dose of the vaccine. She asked should she get the second dose. She got response you should not get the Pfizer-BioNTech COVID-19 Vaccine if you had a severe allergic reaction after a previous dose of the vaccine or if you had a severe allergic reaction to any ingredient of the vaccine. The decision to receive the second dose for any other reason cannot be made by Pfizer. We refer you to speak to your healthcare provider about the risks of the vaccine compared to the risks of potentially not being fully protected against COVID-19 infection. It was reported as PQC was not present. The outcome of the event was unknown. No follow-up attempts are needed; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1306100
Sex: F
Age:
State:

Vax Date: 01/01/2021
Onset Date:
Rec V Date: 05/11/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot:
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data:

Allergies:

Symptom List: Pain in extremity

Symptoms: Tested positive for covid 19; female patient ( in late 70s or early 80s) got the Pfizer covid vaccine first dose in mid Jan and a week later she was tested positive for covid. Caller stated its been 90 days can the patient get her second dose or they need to start all over again; This is a spontaneous report from a contactable pharmacist. An elderly female patient in her late 70s or early 80s received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection), dose 1 via an unspecified route of administration on Jan2021 (Batch/Lot number was not reported) as single dose for covid-19 immunisation. Medical history included neoplasm malignant. Patient was a cancer survivor. The patient's concomitant medications were not reported. On unspecified date two weeks later of the first dose she tested positive for covid 19, she was given an antibody injection in the beginning of February and is now wondering if she still needs the second dose or should she start the series over with the first dose. The patient underwent lab tests and procedures which included sars-cov-2 test: positive. The outcome of the events was reported as unknown. No follow-up attempts are needed; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1306101
Sex: F
Age:
State:

Vax Date: 04/11/2021
Onset Date: 04/01/2021
Rec V Date: 05/11/2021
Hospital:

Vax Type: COVID19
Manufacturer: PFIZER\BIONTECH
Vax Name: COVID19 (COVID19 (PFIZER-BIONTECH))
Lot:
Dose Series: 2
Vax Route:
Vax Site:

Lab Data:

Allergies:

Symptom List: Abdominal pain upper, Abnormal behaviour, Adverse reaction, Anger, Asthma

Symptoms: I feel that the lymph node is swollen, but it's only in the left side, the side that I got the injection; This is a spontaneous report received from a contactable consumer (patient). A female patient of an unspecified age received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; Solution for injection; Lot number: unknown), via an unspecified route of administration on left upper arm on 11Apr2021 as single dose for COVID-19 immunisation. The patient medical history and concomitant medications were not reported. On an unknown date in Apr2021, after vaccination the patient experienced that "it was her left side, right above her clavicle, where she felt that the lymph node was swollen, but it was only in the left side, the side that she got the injection". She stated that "I feel that the lymph node is swollen, but it's only in the left side, the side that I got the injection was coded as vaccination site lymphadenopathy". The patient stated that she was curious about 0.3% of participants experiencing swollen lymph nodes during the clinical study and asked how many participants were enrolled. The outcome of the event was unknown. No follow-up attempts are needed; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1306102
Sex: F
Age:
State: FL

Vax Date: 04/07/2021
Onset Date: 04/13/2021
Rec V Date: 05/11/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot: 039K20A
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data:

Allergies:

Symptom List: Consciousness fluctuating, Crying, Dry skin, Epistaxis, Headache

Symptoms: congestion; fever; headache; sore throat; disorientation; sometimes shortness of breath; had her first dose the 7th/ tested positive on the 13th; This is a Spontaneous report from Pfizer sponsored program. A contactable female consumer (patient) reported that a female patient of unspecified age received first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection) via an unspecified route of administration on 07Apr2021 as a single dose for COVID-19 immunization. The patient's medical history included autoimmune disease and concomitant medications were not reported. On 07Apr2021 she had first dose and scheduled tomorrow with 28Apr2021 for second dose. She tested positive on the 13th of April, tested negative on the 22nd of April and will have another test for Covid-19 by tomorrow. She also had symptoms like congestion, fever, headache, sore throat, disorientation and sometime shortness of breath since 14Apr2021 until now. She is also high-risk person and has autoimmune disease. She is asking if there will be a problem taking the second dose having these symptoms and if she can delay her second dose because her daughter tested positive and will be in quarantine for 10 days. The clinical outcome of the event COVID-19 was recovered, and other events are unknown. No follow-up attempts are needed; information about lot/batch number cannot be obtained. Amendment: This follow-up report is being submitted to amend previously reported Information: Amended and deleted the event "she can delay her second dose because her daughter"/LLT Circumstance or information capable of leading to medication error" and removed "At Risk" classification

Other Meds:

Current Illness:

ID: 1306103
Sex: M
Age:
State:

Vax Date: 04/16/2021
Onset Date: 04/19/2021
Rec V Date: 05/11/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot: 025J20A
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data:

Allergies:

Symptom List: Hypotonia, Lethargy, Respiratory rate decreased, Screaming, Skin warm

Symptoms: A male patient received bnt162b2 (PFIZER-BIONTECH mRNA COVID-19 VACCINE, Formulation: Solution for injection), dose 1 via an unspecified route of administration on 16Apr2021 (Lot number and Expiry date was not reported) as single dose for COVID-19 immunisation. The patient medical history and concomitant medications were not reported. On 16Apr2021, the patient had formed swollen nodes, a swollen kind of region above my left collar bone, patient can't really press into it, it was slightly sore when I press into it. Caller reported his experience after first dose. He recently had first dose on 16Apr2021 and since then well 3 days later he had formed swollen nodes, a swollen kind of region above his left collar bone? He can't really press into it was slightly sore when he pressed into it. Second dose was scheduled for 07May2021. Outcome of the event was unknown. No follow-up attempts are needed; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1306104
Sex: F
Age:
State:

Vax Date: 02/26/2021
Onset Date:
Rec V Date: 05/11/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot: 026LZOA
Dose Series: 1
Vax Route: IM
Vax Site: RA

Lab Data:

Allergies:

Symptom List: Vomiting

Symptoms: her arm was sore near the injection site; then the soreness spread to her shoulder; she can barely move her arm and shoulder; She added she is in "excruciating pain";; it is "terrible" and "debilitating".; her arm pain; This is a spontaneous report from a contactable consumer (reporting for herself). A 79-years-old female patient received second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Batch/Lot number was not reported), via an unspecified route of administration on 26Feb2021 as single dose for covid-19 immunisation. Patient medical history included spinal stenosis from an unknown date and unknown if ongoing. Patient concomitant medications were not reported. Patient persistently asked what to do to manage her symptoms from the Pfizer-BioNTech COVID-19 vaccine. She explained her doctor said he cannot help and has not seen this before. She then threatened to call her lawyer if a doctor or scientist from the company could not assist her. It was stated that patient received the second dose of the Pfizer-BioNTech COVID-19 vaccine on 26Feb2021. She explained a few days after, her arm was sore near the injection site, then the soreness spread to her shoulder and she can barely move her arm and shoulder. She added she was in excruciating pain; it is terrible and debilitating. She took pain medicine for the arthritis in back and described it as spinal stenosis. She mentioned this medication was barely doing something to help with her arm pain. She then specified she also consulted her doctor who prescribed gabapentin and methyl prednisone tablets, which aren't relieving her arm pain. She expressed her concerns on the persistence and intensity of her pain. She asked if her symptoms were reported as side effects to the vaccine. Patient expressed her disappointment on the lack of information provided to manage her symptoms from the Pfizer-BioNTech COVID-19 vaccine. She said she was excited to get this vaccine among the other brand, and now that she is injured from it, she feels like Pfizer should be by her side and thus claims to have help from Pfizer. Outcome of the event her arm pain and her arm were sore near the injection site was not recovered. Outcome of the other events was unknown. No follow-up attempts are needed; information about lot/batch number cannot be obtained

Other Meds:

Current Illness:

ID: 1306105
Sex: F
Age:
State: WI

Vax Date: 04/22/2021
Onset Date: 04/01/2021
Rec V Date: 05/11/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot: 037K20A
Dose Series: 1
Vax Route: SYR
Vax Site: LA

Lab Data:

Allergies:

Symptom List: Headache, Limb discomfort, Nasal congestion

Symptoms: stomach ache; This is a spontaneous report from a contactable consumer (patient) from a Pfizer-sponsored program. A female patient of an unspecified age received bnt162b2 (BNT162B2), dose 2 via an unspecified route of administration on 22Apr2021 (Batch/Lot number was not reported) as SINGLE DOSE for covid-19 immunization. The patient medical history was not reported. The patient's concomitant medications were not reported. The patient received first dose of Pfizer Covid 19 Vaccine on an unknown date. The patient experienced stomach ache in Apr2021. It was reported that the patient had the second dose last Thursday 22Apr2021. She is currently experiencing stomach ache after the dose. She wants to know if this is an adverse event of the vaccine. Outcome of the event was not recovered. No follow-up attempts are needed; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1306106
Sex: F
Age:
State:

Vax Date:
Onset Date: 04/25/2021
Rec V Date: 05/11/2021
Hospital:

Vax Type: COVID19
Manufacturer: PFIZER\BIONTECH
Vax Name: COVID19 (COVID19 (PFIZER-BIONTECH))
Lot:
Dose Series: 1
Vax Route: IM
Vax Site: RA

Lab Data:

Allergies:

Symptom List: Back pain, Cold sweat, Headache, Nausea, Vomiting

Symptoms: rash underneath her armpit; This is a spontaneous report from a non-contactable consumer (patient). A female patient of an unspecified age received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, Batch/Lot number was not reported) via an unspecified route of administration on an unspecified date as single dose for covid-19 immunisation. The patient received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, Batch/Lot number was not reported) via an unspecified route of administration on 27Apr2021 as single dose for covid-19 immunisation. The patient medical history and concomitant medications were not reported. The patient experienced a rash underneath her armpit on 25Apr2021. so she wanted to know if the rash may still be related to the vaccine even if it started to appear days before she got her 2nd dose. She said that aside from that, she felt okay and had no temperature. The outcome of the event was unknown. No follow-up attempts are needed; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1306107
Sex: M
Age:
State: TX

Vax Date: 04/28/2021
Onset Date: 04/29/2021
Rec V Date: 05/11/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot: 025j20-2A
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data:

Allergies:

Symptom List: Injection site swelling, Limb discomfort

Symptoms: Soreness in his lower extremities; This is a spontaneous report from a contactable consumer (patient). A male patient of an unspecified age received the second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE) via an unspecified route of administration on 28Apr2021 as single dose for covid-19 immunisation. The patient medical history and concomitant medications were not reported. The patient experienced soreness in his lower extremities on 29Apr2021. The outcome of the event was unknown. No follow-up attempts are needed; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1306108
Sex: U
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 05/11/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot:
Dose Series: 1
Vax Route: IM
Vax Site: RA

Lab Data:

Allergies:

Symptom List: Chills, Diarrhoea, Fatigue, Feeling abnormal, Headache

Symptoms: vertigo; haven't been able to drive my car in 36 days; This is a spontaneous report from a non-contactable consumer (patient). A patient of unspecified age and gender received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Lot number: Unknown, Expiration date: Un-known), via an unspecified route of administration on unspecified date as single dose for COVID-19 immunization. The patient medical history and concomitant medications were not reported. The patient experienced vertigo and haven't been able to drive my car in 36 days on an unspecified date. Patient asked are you getting calls from people who experience vertigo from the Pfizer BioNTech covid vaccine. I've already called in about this. I am a fairly healthy person. I've been sent for an MRI, MRA and vestibular testing. I found on (site name) 128 people who reporting experiencing vertigo after getting either the Pfizer or Moderna covid vaccine. I haven't been able to drive my car in 36 days. Caller confirmed receiving the Pfizer BioNTech covid vaccine. Response was no information available on the topic of vertigo within current information. Patient underwent lab test and procedures included MRI, MRA and vestibular testing showed unknown result. The outcome of event was unknown. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1306109
Sex: F
Age:
State:

Vax Date: 04/06/2021
Onset Date: 04/06/2021
Rec V Date: 05/11/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot: 037K20A
Dose Series: 1
Vax Route: IM
Vax Site: RA

Lab Data:

Allergies:

Symptom List: Hot flush, Myalgia, Nausea, Tension headache

Symptoms: received first dose April 6th and tested positive for Covid-19.; This is a spontaneous report from a Pfizer sponsored program COVAX US support via contactable consumer (patient, self-reported). A female patient of an unspecified age received first dose of BNT162B2 (PFIZER-BIONTEC COVID-19 mRNA VACCINE, solution for injection, lot number and expiry date were not provided), via an unspecified route of administration, on 06Apr2021, as a single dose for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. The patient's first vaccination was on 06Apr2021 and immediately on the same day, the patient was tested positive for COVID-19. She was supposed to receive second dose on 04May2021 however she was required to quarantine tile 03May2021. She wanted to know if she should still receive the vaccine or what was the protocol for testing positive after receiving the vaccine. Outcome of the event was unknown. No follow-up attempts are needed. No further information is expected.

Other Meds:

Current Illness:

Total 2021 VAERS Injuries: 636,615

Page last modified: 03 October 2021 5:28pm